Canonical Allele Identifier: CA2610723239

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102832512-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832514del , CM000672.2:g.102832514del	GRCh38
NC_000010.10:g.104592271del , CM000672.1:g.104592271del	GRCh37
NC_000010.9:g.104582261del	NCBI36
NG_007955.1:g.10021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1137del (CYP17A1) MANE Select	ENSP00000358903.3:p.Ser380AlafsTer?
ENST00000638190.1:c.834del (CYP17A1)	ENSP00000492539.1:p.Ser279AlafsTer?
ENST00000638272.1:c.681del (CYP17A1)	ENSP00000491508.1:p.Ser228AlafsTer?
ENST00000638971.1:c.1050del (CYP17A1)	ENSP00000492313.1:p.Ser351AlafsTer?
ENST00000639393.1:c.1137del (CYP17A1)	ENSP00000492651.1:p.Ser380AlafsTer?
ENST00000640633.1:n.899del (CYP17A1)
ENST00000647664.1:c.*1545del (WBP1L)	ENSP00000498131.1:n.*1545del
ENST00000369887.3:c.1137del (CYP17A1)	ENSP00000358903.3:p.Ser380AlafsTer?
NM_000102.3:c.1137del (CYP17A1)	NP_000093.1:p.Ser380AlafsTer?
NM_000102.4:c.1137del (CYP17A1) MANE Select	NP_000093.1:p.Ser380AlafsTer?